Posted 7 months ago

No of openings : 05

Job Code: CRAOO1A

Experience: 1 to 4 yrs in Clinical Research Associative.

Job Description :

  • Responsible for conduct of Qualification visit, Site Initiation Visit, Monitoring Visit and Closeouts visit.
  • Would be the first point of contact for Communication with the Investigators and site personnel’s for the study assigned.
  • Coordinate the movement of Laboratory samples if applicable.
  • Ensuring the data entry/CRF filling, following-up visits of subjects as per the protocol.
  • Prepares follow up letters and reports for the respective visits as per the SOPs and share with the site and Sponsor as required.
  • Follow-up with the coordinator for the query resolution.
  • To collect the collated Ethics Committee documents from CTA for EC submission as defined in site SOPs.
  • To ensure that the interim safety reports, interim study reports are provided to EC as per the governed regulatory body.
  • Preparation of power point presentations for investigator meetings and Site Initiation visits.
  • Managing the CRC activities, and training them periodically.

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